Director, GMAL - Pre Approval Access SRP

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.comAs guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.Job Function: Discovery & Pre-Clinical/Clinical DevelopmentJob Sub Function: Clinical Development & Research – MDJob Category:Scientific/TechnologyAll Job Posting Locations:Raritan, New Jersey, United States of AmericaJob Description:Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results.Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.Learn more at The Director, GMAL Pre‑Approval Access – Study Responsible Physician (SRP) is accountable for providing medical and scientific leadership for Oncology Pre‑Approval Access (PAA) programs globally, serving as the primary Study Responsible Physician for PAA activities. In addition to core PAA responsibilities, this role will assume supplementary SRP responsibilities for select Global Medical Affairs (GMAF) clinical trials, ensuring scientific integrity, operational excellence, and compliance across assigned Medical Affairs studies.Primary Responsibilities – Pre‑Approval Access (PAA) SRP· Serve as Study Responsible Physician (SRP) for assigned PAA programs and conduct medical review of individual patient requests.· Review HCP submissions to determine patient eligibility based on protocol criteria and benefit–risk considerations.· Partner with GMALs and CDTLs on complex or exceptional eligibility cases.· Maintain expertise in clinical trial protocols, treatment guidelines, and PAA criteria.· Collaborate with Post Approval Delivery Unit colleagues to track cases in the Global Trial System.· Ensure compliance with SOPs, GCP, regulatory requirements, and internal PAA policies.· Partner with regional Medical Affairs teams to obtain additional clinical context as needed.Supplementary Responsibilities – GMAF Clinical Trial SRP· Provide medical and scientific oversight for assigned GMAF-sponsored clinical trials.· Review and approve study protocols, informed consent forms, and medical review plans.· Serve as primary medical contact for investigators and internal study teams.· Support regulatory, safety, and compliance activities.· Contribute to analysis, interpretation, and dissemination of study results.· Ensure alignment with the Integrated Evidence Generation Plan (IEGP).Qualifications· MD (or equivalent medical degree) required· Oncology clinical experience required· Board certification in Oncology preferred· Minimum 5 years experience in Medical Affairs or clinical research· Prior experience as SRP strongly preferredAdditional InformationApproximately 10% domestic and international travel may be required. This role is remote-based with periodic travel to global meetings.The anticipated base pay range for this position is $199,000 - $343,000.The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/performance year. Bonuses are awarded at the Company’s discretion on an individual basis.Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.Employees may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).This position is eligible to participate in the Company’s long-term incentive program.Employees are eligible for the following time off benefits:Vacation – up to 120 hours per calendar yearSick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar yearHoliday pay, including Floating Holidays – up to 13 days per calendar year of Work, Personal and Family Time - up to 40 hours per calendar yearAdditional information can be found via the following link: The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please contact us via or contact AskGS to be directed to your accommodation resource.Required Skills:Preferred Skills:Business Savvy, Clinical Research and Regulations, Clinical Trials, Collaborating, Consulting, Data Management and Informatics, Design Mindset, Drug Discovery Development, Industry Analysis, Innovation, Market Research, Regulatory Affairs Management, Research Ethics, Scientific Evaluation, Scientific Research, Stakeholder Management, Strategic AnalysisThe anticipated base pay range for this position is :$199,000.00 - $343,850.00Additional Description for Pay Transparency:SummaryLocation: Raritan, New Jersey, United States of AmericaType: Full time